Insulin-IGF signaling affects cell transformation in the BALB/c 3T3 cell model

被引:8
作者
Poburski, Doerte [1 ]
Leovsky, Christiane [1 ]
Boerner, Josefine Barbara [1 ]
Szimmtenings, Luisa [1 ]
Ristow, Michael [1 ,2 ]
Glei, Michael [1 ]
Thierbach, Rene [1 ]
机构
[1] Friedrich Schiller Univ Jena, Inst Nutr, Dornburger Str 24, D-07743 Jena, Germany
[2] Swiss Fed Inst Technol, Energy Metab Lab, Schorenstr 16, CH-8603 Schwerzenbach, Switzerland
关键词
GROWTH-FACTOR RECEPTOR; I RECEPTOR; INHIBITOR OSI-906; DUAL INHIBITOR; BREAST-CANCER; RAS-ERK; PATHWAY; EXPRESSION; CARCINOMA; TARGET;
D O I
10.1038/srep37120
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The increased cancer mortality of diabetes type 2 patients is most likely an evidence of the tight connection between tumor development and energy metabolism. A major focus of today's research is still the identification of key proteins of both diseases and the development of corresponding inhibitors. In this study we combined the two-stage BALB/c-3T3 cell transformation assay (BALB-CTA) with the IR/IGF-1R inhibitor OSI-906 (linsitinib) and analyzed alterations in protein activity and energy parameters in non-transformed as well as transformed cells. OSI-906 successfully inhibited the phosphorylation of IR/IGF-1R and decreased cell growth in non-transformed cells. In the BALB-CTA, a permanent treatment with OSI-906 reduced cellular transformation dose-dependently, whereas a temporary treatment gave evidence for a preventive effect in the promotion phase. Furthermore, even though several key proteins were affected, it was possible to show that the phosphorylation of GSK3, Erk 1/2 and the S6 protein are not crucial for the cell foci reducing effect of OSI-906. Taken together, the BALB-CTA confirmed results of OSI-906 from animal studies and enhanced the knowledge of its mode of action. Therefore, the BALB-CTA offers the opportunity to analyze alterations in the transformation process more precisely and will be helpful to identify effective cancer treatments.
引用
收藏
页数:12
相关论文
共 69 条
[61]   MEASUREMENT OF PROTEIN USING BICINCHONINIC ACID [J].
SMITH, PK ;
KROHN, RI ;
HERMANSON, GT ;
MALLIA, AK ;
GARTNER, FH ;
PROVENZANO, MD ;
FUJIMOTO, EK ;
GOEKE, NM ;
OLSON, BJ ;
KLENK, DC .
ANALYTICAL BIOCHEMISTRY, 1985, 150 (01) :76-85
[62]   Lithium reduces tumorigenic potential in response to EGF signaling in human colorectal cancer cells [J].
Vidal, Flavia ;
De Araujo, Wallace Martins ;
Cruz, Andre L. S. ;
Tanaka, Marcelo Neves ;
Viola, Joao P. B. ;
Morgado-Diaz, Jose A. .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2011, 38 (05) :1365-1373
[63]   Embryonic Origin and Remodeling of the Urinary and Digestive Outlets [J].
Wang, Chen ;
Wang, JingYing ;
Borer, Joseph G. ;
Li, Xue .
PLOS ONE, 2013, 8 (02)
[64]   Yin and yang of 4E-BP1 in cancer [J].
Wang, Ren ;
Ganesan, Shridar ;
Zheng, X. F. Steven .
CELL CYCLE, 2016, 15 (11) :1401-1402
[65]   Inhibition of insulin-like growth factor-I receptor (IGF-IR) signaling and tumor cell growth by a fully human neutralizing anti-IGF-IR antibody [J].
Wang, Y ;
Hailey, J ;
Williams, D ;
Wang, YL ;
Lipari, P ;
Malkowski, M ;
Wang, XY ;
Xie, L ;
Li, GH ;
Saha, D ;
Lam, W ;
Ling, W ;
Cannon-Carlson, S ;
Greenberg, R ;
Ramos, RA ;
Shields, R ;
Presta, L ;
Brams, P ;
Bishop, WR ;
Pachter, JA .
MOLECULAR CANCER THERAPEUTICS, 2005, 4 (08) :1214-1221
[66]   ORIGIN OF CANCER CELLS [J].
WARBURG, O .
SCIENCE, 1956, 123 (3191) :309-314
[67]  
Warburg O., 1925, KLIN WOCHENSCHR, V4, P534, DOI DOI 10.1007/BF01726151
[68]   Diabetes and Cancer: a Review of Current Knowledge [J].
Wojciechowska, J. ;
Krajewski, W. ;
Bolanowski, M. ;
Krecicki, T. ;
Zatonski, T. .
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2016, 124 (05) :263-275
[69]   Epithelial-Mesenchymal Transition Predicts Sensitivity to the Dual IGF-1R/IR Inhibitor OSI-906 in Hepatocellular Carcinoma Cell Lines [J].
Zhao, Hui ;
Desai, Vidhi ;
Wang, Jian ;
Epstein, David M. ;
Miglarese, Mark ;
Buck, Elizabeth .
MOLECULAR CANCER THERAPEUTICS, 2012, 11 (02) :503-513